A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603232



Internal ID21795279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84672080..84672270hg38UCSC Ensembl
chr15:85215311..85215501hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6035508
Supporting Variants
Samples
Known GenesSEC11A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603232
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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